JP2871099B2 - Flexible polyvinyl chloride product and method for producing the same - Google Patents
Flexible polyvinyl chloride product and method for producing the sameInfo
- Publication number
- JP2871099B2 JP2871099B2 JP51750995A JP51750995A JP2871099B2 JP 2871099 B2 JP2871099 B2 JP 2871099B2 JP 51750995 A JP51750995 A JP 51750995A JP 51750995 A JP51750995 A JP 51750995A JP 2871099 B2 JP2871099 B2 JP 2871099B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- glove
- mold
- film
- plastisol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000004800 polyvinyl chloride Substances 0.000 title claims abstract description 33
- 229920000915 polyvinyl chloride Polymers 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title description 9
- 229920001944 Plastisol Polymers 0.000 claims abstract description 33
- 239000004999 plastisol Substances 0.000 claims abstract description 33
- 229920002635 polyurethane Polymers 0.000 claims abstract description 29
- 239000004814 polyurethane Substances 0.000 claims abstract description 29
- 239000012748 slip agent Substances 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 23
- 229920000728 polyester Polymers 0.000 claims abstract description 21
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 239000000843 powder Substances 0.000 claims abstract description 16
- 239000000839 emulsion Substances 0.000 claims abstract description 8
- 238000007598 dipping method Methods 0.000 claims abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 19
- 239000000463 material Substances 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 239000004014 plasticizer Substances 0.000 claims description 12
- 239000005997 Calcium carbide Substances 0.000 claims description 8
- 239000002421 finishing Substances 0.000 claims description 8
- CLZWAWBPWVRRGI-UHFFFAOYSA-N tert-butyl 2-[2-[2-[2-[bis[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]-5-bromophenoxy]ethoxy]-4-methyl-n-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]anilino]acetate Chemical compound CC1=CC=C(N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(OCCOC=2C(=CC=C(Br)C=2)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)=C1 CLZWAWBPWVRRGI-UHFFFAOYSA-N 0.000 claims description 8
- 238000009826 distribution Methods 0.000 claims description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 claims description 6
- 239000005909 Kieselgur Substances 0.000 claims description 5
- 239000011324 bead Substances 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 4
- 230000007306 turnover Effects 0.000 claims description 4
- 239000002518 antifoaming agent Substances 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000007900 aqueous suspension Substances 0.000 claims description 2
- 150000005690 diesters Chemical class 0.000 claims description 2
- 239000000375 suspending agent Substances 0.000 claims description 2
- 150000001278 adipic acid derivatives Chemical class 0.000 claims 2
- 150000003022 phthalic acids Chemical class 0.000 claims 2
- 239000002562 thickening agent Substances 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- 239000000080 wetting agent Substances 0.000 claims 2
- 238000004026 adhesive bonding Methods 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000004806 packaging method and process Methods 0.000 claims 1
- 125000005498 phthalate group Chemical class 0.000 claims 1
- 229920006264 polyurethane film Polymers 0.000 claims 1
- 239000010410 layer Substances 0.000 description 56
- -1 phthalic acid ester Chemical class 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 239000013536 elastomeric material Substances 0.000 description 5
- 229920006173 natural rubber latex Polymers 0.000 description 5
- 239000011236 particulate material Substances 0.000 description 5
- 229920000126 latex Polymers 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 229920002261 Corn starch Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000008120 corn starch Substances 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 241000725303 Human immunodeficiency virus Species 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000000172 allergic effect Effects 0.000 description 2
- 208000010668 atopic eczema Diseases 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000008037 PVC plasticizer Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000011325 microbead Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/02—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
- B29C41/14—Dipping a core
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/04—Macromolecular materials
- A61L31/048—Macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/08—Materials for coatings
- A61L31/10—Macromolecular materials
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D19/00—Gloves
- A41D19/0055—Plastic or rubber gloves
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/252—Glass or ceramic [i.e., fired or glazed clay, cement, etc.] [porcelain, quartz, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/259—Silicic material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
- Y10T428/3158—Halide monomer type [polyvinyl chloride, etc.]
Landscapes
- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Surgery (AREA)
- Vascular Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Gloves (AREA)
- Moulding By Coating Moulds (AREA)
- Laminated Bodies (AREA)
- Materials For Medical Uses (AREA)
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 本発明は柔軟性製品に関し、より特定すれば、粉末を
含まないポリ塩化ビニル製試験用手袋およびその製造方
法に関する。Description: FIELD OF THE INVENTION The present invention relates to flexible products, and more particularly, to powder-free polyvinyl chloride test gloves and a method of making the same.
発明の背景 柔軟性防水手袋は医薬業にとって重要な道具である。
古典的なこれらの手袋は、手形の型をラテックスに浸
け、ラテックスを連続フィルムに硬化し、次に、型から
手袋を取り出すことにより、天然ゴムラテックスから成
形された。天然ゴムから成形された手袋は先天的に自己
接着するため、浸漬前に型上に粉末の離型剤を適用して
成形された手袋が型に接着しないようにする必要があ
る。BACKGROUND OF THE INVENTION Flexible waterproof gloves are an important tool for the pharmaceutical industry.
These classic gloves were molded from natural rubber latex by dipping a handprint mold into latex, curing the latex into a continuous film, and then removing the glove from the mold. Since gloves molded from natural rubber are self-adhesive innately, it is necessary to apply a powder release agent on the mold before dipping so that the molded glove does not adhere to the mold.
天然ゴムラテックスは高価であり、アレルギーの潜在
性を有しうる。合成ポリマーの開発により、天然合成ラ
テックス以外の材料から柔軟性フィルム手袋を生産する
ことが可能になった、ポリウレタンおよびアクリレート
は天然ゴムに成形されることができ、そしてポリ塩化ビ
ニル(PVC)はプラスチゾルとして製造できるため天然
ゴムラテックスと実質的に同様な特性を有するフィルム
手袋が製造できる。これらのビニル手袋の代表的なもの
は、Tru−Touch(登録商標)(ベクトンディッキンソン
社、フランクリンレイクス、ニュージャージー)であ
る。Natural rubber latex is expensive and can have allergic potential. The development of synthetic polymers has made it possible to produce flexible film gloves from materials other than natural synthetic latex, polyurethanes and acrylates can be molded into natural rubber, and polyvinyl chloride (PVC) is a plastisol Thus, a film glove having substantially the same properties as natural rubber latex can be manufactured. A representative of these vinyl gloves is Tru-Touch® (Becton Dickinson, Franklin Lakes, NJ).
PVCプラスチゾルから製造された手袋も自己接着性で
あり、且つ、ラテックス手袋において用いられたのと同
様な離型剤が、これらのPVC手袋に用いられる。Gloves made from PVC plastisols are also self-adhesive, and release agents similar to those used in latex gloves are used for these PVC gloves.
ヒト免疫不全ウイルス(HIV)の到来と共に、フィル
ム手袋はよりしばしばそしてより頻繁に実験室の労働者
および医者により着用されている。以前は必要な時のみ
着用していた多くの労働者は、今はほぼ連続的に着用す
る必要がある。この増加した使用の必要性により、使用
者集団が手袋により多くさらされることとなり、そして
手袋の成形に用いられる幾つかの物質および手袋に用い
られる粉末離型剤へのアレルギー性感受性の例が報告さ
れてきた。さらに、幾つかの応用に関して、手袋上の粉
末離型剤の存在は、手袋を着用する際に使用者がふるま
う手順を妨害する。天然ゴムラテックス上の粉末離型剤
の排除に関する幾つかの報告があり、例えば天然ゴムラ
テックスのハロゲン化のような化学処理の利用または手
袋表面への潤滑剤の付着等である。With the advent of the human immunodeficiency virus (HIV), film gloves are more often and more often worn by laboratory workers and doctors. Many workers who used to wear only when needed now need to wear it almost continuously. This increased need for use results in greater exposure of the user population to gloves, and reports of examples of allergic susceptibility to some substances used in glove molding and powder release agents used in gloves It has been. In addition, for some applications, the presence of a powder release agent on the glove interferes with the user's behaving procedures when wearing the glove. There have been several reports on the elimination of powder release agents on natural rubber latex, for example the use of chemical treatments such as halogenation of natural rubber latex or the adhesion of lubricants to glove surfaces.
アンセル(Ansell)らに対する米国特許第5,088,125
号はエラストマー手袋を教示しているが、良好な着用
(donning)特性は例えばタルクのような着用助剤(don
ning agent)の必要なしに、そして重合法による内部ラ
ミネートの生成なしに得られる。該特許は、さらに、イ
オン性ポリウレタンおよび該イオン性ポリウレタンより
大きな粒子サイズを有する分散した第二のポリマーから
なる、第二のエラストマー物質でコートされた手袋の手
に接触する表面を有する、第一の柔軟性エラストマー物
質から成形された手袋を教示している。ポリウレタンよ
りも大きな粒子サイズを有する有機ポリマー材料のみが
分散した粒子性材料として示唆される。U.S. Patent No. 5,088,125 to Ansell et al.
Teaches elastomeric gloves, but has good donning properties, such as talc.
ning agent) and without the production of internal laminates by the polymerization method. The patent further discloses a glove coated with a second elastomeric material comprising a ionic polyurethane and a dispersed second polymer having a larger particle size than the ionic polyurethane, the glove having a hand-contacting surface. Teaches gloves molded from a flexible elastomeric material. Only organic polymer materials having a larger particle size than polyurethane are suggested as dispersed particulate material.
ストッカム(Stockum)への米国特許第4,143,109号
は、着用者に密着性をもって均一に適合し、そして付加
的な潤滑剤の使用なしに着用可能な医療用手袋の製造方
法を教示している。該特許は、エラストマー物質の外層
を有する医療用手袋を教示している。エラストマー物質
の独立した内層は外層に結合しており、そして粒状性物
質は内層内に安全に埋められてランダムに分散されてい
る。粒状性物質は内部の皮膚接触層に一部露出している
ことが好ましく、それにより、サイズおよび形態におい
て内部表面上に突起を形成するように、そして粉末を用
いる手袋と同様な量的分布で内部表面上に広がる。該特
許は、ポリウレタンのマイクロビーズ並びに他のポリマ
ーの使用を教示しており、両者は天然に存在しており人
造される。コーンスターチおよび架橋コーンスターチは
特に適切な材料であり且つ所望の潤滑特性を有するもの
として教示されている。U.S. Pat. No. 4,143,109 to Stockum teaches a method of making medical gloves that are coherent and uniform to the wearer and that can be worn without the use of additional lubricants. The patent teaches a medical glove having an outer layer of an elastomeric material. A separate inner layer of elastomeric material is bonded to the outer layer, and the particulate material is safely embedded within the inner layer and randomly dispersed. The particulate material is preferably partially exposed to the inner skin contact layer, thereby forming protrusions on the inner surface in size and morphology, and with a quantitative distribution similar to powdered gloves. Spreads on the inner surface. The patent teaches the use of microbeads of polyurethane as well as other polymers, both of which are naturally occurring and artificial. Corn starch and crosslinked corn starch are taught as being particularly suitable materials and having desired lubricating properties.
上記引用された特許の教示は離型剤を必要とせずに着
用可能となる手袋を提供するための幾つかの手袋製造方
法を当業者に提供するが、部分的に露出した埋蔵物質の
潤滑特性にのみ依存することなく、粉末を用いずに着用
可能であって且つ効果的に製造できるビニル手袋の要求
がいまだ存在する。Although the teachings of the above-cited patents provide those skilled in the art with several glove manufacturing methods to provide gloves that can be worn without the need for a release agent, the lubricating properties of partially exposed deposits There is still a need for vinyl gloves that can be worn without powder, without relying solely on and that can be effectively manufactured.
発明の概要 柔軟性製品は、可塑化ポリ塩化ビニルからなる第一の
層および第一の層に接着した第二の層を含む。第二の層
はポリエステルポリウレタン、スリップ剤および仕上剤
を含む。SUMMARY OF THE INVENTION A flexible product includes a first layer of plasticized polyvinyl chloride and a second layer adhered to the first layer. The second layer includes a polyester polyurethane, a slip agent and a finish.
該製品は医療に有用な2層手袋であることが好まし
い。手袋は可塑化ポリ塩化ビニル樹脂のフィルムとして
形成された第一の患者接触層およびポリエステルポリウ
レタンのフィルムで形成された第二の使用者接触層を含
む。患者接触層は、可塑剤例えばフタル酸エステル、ア
ジピン酸エステル等により可塑化された縮合ポリ塩化ビ
ニルゲルから形成されることが好ましい。The product is preferably a medically useful two-layer glove. The glove includes a first patient contact layer formed as a film of a plasticized polyvinyl chloride resin and a second user contact layer formed of a film of polyester polyurethane. The patient contact layer is preferably formed from a condensed polyvinyl chloride gel plasticized with a plasticizer such as a phthalic acid ester, an adipic acid ester and the like.
使用者接触層は、きめを有する表面を提供するスリッ
プ剤および仕上剤を含み、それにより、使用者接触層は
それ自体で使用者の皮膚を滑り、即ち本発明の手袋を粉
末の必要なしに着用可能とする。The user contact layer includes a slip agent and a finish that provides a textured surface, whereby the user contact layer slides on the user's skin by itself, i.e., without the need for powders of the gloves of the present invention. Can be worn.
医療において有用な本発明の手袋を製造するための方
法は、表面を有する清潔な手形の型をポリ塩化ビニルプ
ラスチゾルを含む第一浴槽に浸す。プラスチゾルフィル
ムを型の表面上で形成し、次に型を第一浴槽から取り出
す。その表面上に第一フィルムを有する型を加熱してプ
ラスチゾルをゲルにして縮合する。その表面上に第一フ
ィルムを有する型は、次に冷やされ、そしてポリエステ
ルポリウレタン、スリップ剤および仕上剤を含む第二浴
槽を浸す。次にポリエステルポリウレタン、スリップ剤
および仕上剤の第二フィルムを第一フィルム上に形成
し、そして第一フィルムおよび第二フィルムをその表面
上に有する型を加熱乾燥して第一フィルムと第二フィル
ムを接着する。これにより、型の表面上に2層のユニッ
ト構造が形成される。次に、型の表面上のユニット構造
上にめくり返し(cuff)を形成する。めくり返すことに
より型の表面からユニット構造をはぎとり、それによ
り、外部表面上に患者接触層および内容表面上に使用者
接触層を有する手袋が形成される。A method for making gloves of the present invention useful in medicine is to dip a clean handprint mold having a surface into a first bath containing polyvinyl chloride plastisol. A plastisol film is formed on the surface of the mold, and the mold is then removed from the first bath. The mold having the first film on its surface is heated to gel the plastisol and condense. The mold with the first film on its surface is then cooled and soaks a second bath containing the polyester polyurethane, slip agent and finish. Next, a second film of the polyester polyurethane, slip agent and finishing agent is formed on the first film, and the mold having the first film and the second film on its surface is dried by heating to form the first film and the second film. Glue. This forms a two-layer unit structure on the surface of the mold. Next, a cuff is formed on the unit structure on the surface of the mold. Turning over peels the unit structure from the surface of the mold, thereby forming a glove having a patient contact layer on the outer surface and a user contact layer on the content surface.
医療に有用な手袋の製造方法は、手形の型の外部表面
上にポリ塩化ビニルのプラスチゾルの第一層を形成する
ことを含む。次に、ポリエステルポリウレタン、スリッ
プ剤および仕上剤の第二層を型上の第一層上に接着して
形成する。A method of making a medically useful glove includes forming a first layer of a plastisol of polyvinyl chloride on the exterior surface of a bill mold. Next, a second layer of polyester polyurethane, slip agent and finish is adhered to the first layer on the mold to form.
本発明の手袋は極めて柔軟性であり、優秀な伸びおよ
び強度を有するが、優秀な触質感受性を付与する厚さを
持ち合わせる。さらに、使用者接触層内のスリップ剤お
よび仕上剤の存在により型からの手袋のはぎとりおよび
めくり返しが容易になり、それにより粉末を用いない手
袋において以前は不可能であった製造効率が達成され
る。スリップ剤および仕上剤により手袋は実質的に自己
接着しなくなり、そして表面上の粉末を必要とせずに使
用者が手袋を着用できる。The gloves of the present invention are extremely flexible, have excellent elongation and strength, but have a thickness that provides excellent tactile sensitivity. In addition, the presence of slip agents and finishes in the user contact layer facilitates stripping and flipping of gloves from the mold, thereby achieving previously impossible manufacturing efficiencies in powderless gloves. You. The slip and finish substantially eliminate glove self-adhesion and allow the user to wear the glove without the need for powder on the surface.
図面の簡単な説明 図1は、粉末を使用しない本発明の手袋を形成する工
程の模式図である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic view of a step of forming a glove of the present invention without using a powder.
図2aおよび2bは、従来技術の手袋の表面の断面の模式
図(2a)および本発明の手袋の断面および表面のミクロ
写真(2b)である。FIGS. 2a and 2b are a schematic view (2a) of a cross section of the surface of a glove of the prior art and a microphotograph (2b) of the cross section and surface of the glove of the present invention.
詳細な説明 本発明は多くの異なる形態の態様により満たされる
が、本発明の開示は発明の原理の例示として考えられ且
つ記載された態様に本発明を限定する意図でないという
理解と共に、本発明の好ましい態様を詳細に記載する。DETAILED DESCRIPTION While the present invention is fulfilled by many different embodiments, it is to be understood that the present disclosure is to be understood as illustrative of the principles of the invention and is not intended to limit the invention to the described embodiments. Preferred embodiments are described in detail.
本発明によれば、可塑化ポリ塩化ビニル(PVC)また
はPVCコポリマーから形成される第一層および第一層に
接着したポリエステルポリウレタン、スリップ剤および
仕上剤の第二層を有する柔軟性製品が製造されうる。According to the present invention, a flexible product having a first layer formed of plasticized polyvinyl chloride (PVC) or a PVC copolymer and a second layer of polyester polyurethane, a slip agent and a finish bonded to the first layer is produced. Can be done.
医療に有用な手袋は、可塑化ポリ塩化ビニル(PVC)
またはPVCコポリマーから形成される第一患者接触層、
および第一層に接着した、ポリエステルポリウレタンか
ら形成される使用者に接触する第二層を含む。本発明の
手袋は、使用者接触層中にスリップ剤および仕上剤を含
むことが好ましい。スリップ剤および仕上剤の存在によ
り使用者接触層自体がスライドし、そして使用者の皮膚
と手袋表面の間の接触領域を実質的に減らすミクロなざ
らつきを有する使用者接触層表面を提供し、それによ
り、現在のPVC手袋に必要とされる粉末を用いずに容易
に手袋が着用される。Medically useful gloves are plasticized polyvinyl chloride (PVC)
Or a first patient contact layer formed from a PVC copolymer,
And a second user contact layer formed from polyester polyurethane adhered to the first layer. The glove of the present invention preferably contains a slip agent and a finishing agent in the user contact layer. The user contact layer itself slides due to the presence of the slip agent and the finish, and provides a user contact layer surface with micro-texture that substantially reduces the contact area between the user's skin and the glove surface. Allows gloves to be easily worn without the powders required for current PVC gloves.
粉末を用いる手袋において、粉末は、手袋表面を分離
して互いの接着を阻害し、並びに接触領域を減らすこと
により使用者の皮膚に対して手袋表面をスライドさせる
潤滑剤としての機能を有する。ストッカム(Stockum)
への米国特許第4,143,109号は、エラストマー手袋基質
がエラストマー物質中に粒子懸濁液を有する基質層上の
第二層を有することを教示している。ストッカムは、粒
子が第二層の厚さよりも大きいサイズであることによ
り、外部に向かって露出する部分を有する表面を通して
盛り上がらせるべきであり、それにより粒子の潤滑特性
は表面をスリップしやすくするのに役立つことを教示し
ている。該特許はさらに、粒子が生理学的に不活性であ
り、滑らかな表面でありそして低い摩擦係数を有するこ
とが好ましいことを教示している。ストッカムにより教
示された好ましい材料はエピクロロヒドリンで架橋され
たコーンスターチであり、潤滑性粉末として多くの粉末
手袋において用いられている材料である。In gloves that use powder, the powder acts as a lubricant that separates the glove surface and inhibits adhesion to each other, as well as sliding the glove surface against the user's skin by reducing the area of contact. Stockum (Stockum)
U.S. Pat. No. 4,143,109 teaches that an elastomeric glove substrate has a second layer over the substrate layer having a particle suspension in the elastomeric material. The stocker should be raised through the surface with the parts that are exposed to the outside due to the size of the particles being greater than the thickness of the second layer, so that the lubricating properties of the particles make the surface easier to slip Teaches you to help. The patent further teaches that the particles are preferably physiologically inert, have a smooth surface, and have a low coefficient of friction. The preferred material taught by Stockham is corn starch crosslinked with epichlorohydrin, a material used in many powdered gloves as a lubricating powder.
驚くことに、本発明は、研磨剤として市販されて用い
られている材料、例えば炭化カルシウム、合成非晶質シ
リケート、シリケート、珪藻土およびガラスビーズを利
用することができる。本発明において、使用者接触層に
おいて仕上剤として用いられる粒ぞろいの物質は実質的
にポリエステルポリウレタンでコートされるが、部分的
に露出されてそのため潜在的に除去可能とすることより
むしろ、表面が実質的にスムーズになるのを妨害し、即
ち手袋表面と使用者の皮膚の間の接触を実質的に減らし
て摩擦を減らすことにより、スリップ特性が増加した表
面を提供する。Surprisingly, the present invention can utilize materials that are used commercially as abrasives, such as calcium carbide, synthetic amorphous silicates, silicates, diatomaceous earth, and glass beads. In the present invention, the assorted material used as a finish in the user contact layer is substantially coated with a polyester polyurethane, but rather than having a partially exposed and thus potentially removable surface, It provides a surface with increased slip properties by preventing smoothing, i.e., substantially reducing contact between the glove surface and the user's skin and reducing friction.
ASTM試験法D−1894(引用により本明細書の一部をな
す)を用いた静摩擦係数(COF)のピークに関して、幾
つかの市販の粉末不含手袋のサンプルを本発明と共に試
験した。試験装置(カイエネス(Kayeness)D5095D)を
スレッド(sled)上で15.2cm/分で190グラムに設定し
た。表1は、周囲温度(約23℃から約30℃の間)および
上昇温度(約65℃から約70℃)における摩擦係数および
標準偏差(括弧内)を示す。この実験の目的において、
周囲温度および上昇温度における温度の偏差は重要では
ない。Several commercially available powder-free glove samples were tested with the present invention for the coefficient of static friction (COF) peaks using ASTM test method D-1894, which is incorporated herein by reference. The test apparatus (Kayeness D5095D) was set on a sled to 190 grams at 15.2 cm / min. Table 1 shows the coefficient of friction and standard deviation (in parentheses) at ambient temperature (between about 23 ° C. and about 30 ° C.) and elevated temperature (about 65 ° C. to about 70 ° C.). For the purpose of this experiment,
Temperature deviations at ambient and elevated temperatures are not significant.
この結果は、試験された市販の製品に比して本発明が
低い摩擦係数を有することを示す。さらに、本発明の第
二層中の酸化ポリエチレンスリップ剤の存在が上昇温度
における実質的に低い摩擦係数を提供すると信じられ
る。上昇温度におけるこの低い摩擦係数は型からの本発
明の手袋の迅速なはぎとりおよびめくり返しを促進す
る。 This result indicates that the present invention has a lower coefficient of friction as compared to the commercial products tested. Further, it is believed that the presence of the oxidized polyethylene slip agent in the second layer of the present invention provides a substantially lower coefficient of friction at elevated temperatures. This low coefficient of friction at elevated temperatures promotes rapid stripping and flipping of the gloves of the present invention from the mold.
以下のリストの材料は、本発明の好ましい態様の代表
的実施例において用いるのに適切であることが見いださ
れた。これらの試薬および以下の実施例は本発明、即ち
好ましい態様における本発明の方法および製造工程、医
療における使用に適切な手袋を例示するものであって限
定するものではない。The materials in the following list have been found to be suitable for use in representative embodiments of the preferred embodiments of the invention. These reagents and the following examples are illustrative, but not limiting, of the present invention, i.e., the methods and processes of the present invention in a preferred embodiment, gloves suitable for use in medicine.
I.ポリ塩化ビニル(PVC)またはPVCコポリマー分散樹脂 約0.7から約1.5の極限粘度数(ASTM D−1243方法A) II.PVCの可塑剤 III.安定剤 適切な安定剤はエポキシ化タル油、エポキシ化大豆
油、遷移金属セッケン等である。I. Intrinsic viscosity of about 0.7 to about 1.5 (ASTM D-1243 Method A) II.PVC plasticizer III. Stabilizers Suitable stabilizers are epoxidized tall oil, epoxidized soybean oil, transition metal soap and the like.
iV,粘度修飾剤 V.仕上剤 V.スリップ剤 VI.フローエンハンサー VII.ポリエステルポリウレタンエマルジョン VIII.消泡剤 IX.表面活性剤(修飾脂肪族ポリエーテル) 実施例 本発明の好ましい態様を製造するための模式図を参照
すると(図1)、外部表面に関してヒトの手形を有する
清潔な型を加熱して温度を約70℃から約95℃にしてPVC
プラスチゾルまたはプラスチゾルとしてマレイン酸エス
テルまたはアクリル酸エステル等を含むPVCコポリマー
を含有する約35℃から約45℃に維持された第一浴槽に型
を浸ける。PVCプラスチゾルは極限粘度数約0.7から約1.
5(ASTM D−1243方法A)を有するポリ塩化ビニル分散
樹脂;可塑剤、好ましくは7から10の炭素原子鎖を有す
るフタル酸またはアジピン酸モノまたはジエステルおよ
びそのブレンド;安定剤成分および色素を含むことが好
ましい。プラスチゾルは粘度修飾剤、消泡剤等も含んで
よい。第一浴槽中での型の滞留時間、浴槽の固体含有率
および温度すべてが形成されるフィルムの厚さに影響す
る。好ましくは、滞留時間は、プラスチゾルが約0.03mm
から約0.14mmの厚さにフィルム形成されるのに十分な時
間であって、所望のフィルム厚および手袋の適用意図に
依存する。可塑剤に対する樹脂の比率は約0.8:1から約
1.2:1が好ましい。 iV, viscosity modifier V. Finishing agent V. Slip agent VI. Flow enhancer VII. Polyester polyurethane emulsion VIII. Antifoaming agent IX. Surfactant (modified aliphatic polyether) EXAMPLES Referring to the schematic diagram for manufacturing a preferred embodiment of the present invention (FIG. 1), a clean mold having a human handprint on an external surface is heated to a temperature of about 70 ° C. to about 95 ° C. and PVC.
The mold is immersed in a first bath maintained at about 35 ° C. to about 45 ° C. containing a plastisol or a PVC copolymer containing maleic acid ester or acrylic acid ester as the plastisol. PVC plastisol has an intrinsic viscosity of about 0.7 to about 1.
5 (ASTM D-1243 Method A); polyvinyl chloride dispersion resin; plasticizer, preferably phthalic or adipic mono- or diesters having a chain of 7 to 10 carbon atoms and blends thereof; including stabilizer component and pigment Is preferred. The plastisol may also include viscosity modifiers, defoamers, and the like. The residence time of the mold in the first bath, the solids content of the bath and the temperature all affect the thickness of the film formed. Preferably, the residence time is about 0.03 mm for plastisol
This is a time sufficient to form a film from about 0.14 mm to about 0.14 mm, depending on the desired film thickness and glove application intent. The ratio of resin to plasticizer is from about 0.8: 1 to about
1.2: 1 is preferred.
次に、その表面上にプラスチゾルを有する型を第一浴
槽から取り出し、そしてオーブンに入れてゲル化させて
プラスチゾルフィルムを縮合する。オーブンの条件およ
び滞留時間はフィルムの温度を上昇させて約160℃から
約195℃にするのに十分であることが好ましい。The mold with the plastisol on its surface is then removed from the first bath and placed in an oven to gel to condense the plastisol film. Preferably, the oven conditions and residence time are sufficient to raise the temperature of the film from about 160 ° C to about 195 ° C.
ゲル化および縮合工程は、プラスチゾル化合物を液体
状態から実質的に固体の状態にする。ゲル化および縮合
工程は、上昇温度における可塑剤による樹脂の溶媒和を
含む。可塑剤は周囲温度においては劣った溶剤である
が、しかし、上昇温度においては続く物理特性の発現、
伸び、引張強度、および弾性を伴って樹脂を溶解または
縮合する。本発明においては、第一浴槽中のプラスチゾ
ルはPVC樹脂粒子を湿潤および懸濁させるのに十分な温
度であるがゲル化および縮合が起こる温度以下に保持さ
れなければならない。その表面上に液体プラスチゾルフ
ィルムを有する型を浴槽から取り出したら、排水をして
次にオーブンを加熱してゲル化および縮合を起こさせ
る。これらの工程のための正確な時間および温度は、特
定の樹脂、可塑剤、樹脂/可塑剤比率、所望のフィルム
厚、および手袋製造のための所望の処理量に依存する。The gelling and condensation steps bring the plastisol compound from a liquid state to a substantially solid state. The gelling and condensation steps involve solvation of the resin with a plasticizer at elevated temperatures. Plasticizers are poor solvents at ambient temperature, however, at elevated temperatures, they continue to exhibit physical properties,
Dissolves or condenses resins with elongation, tensile strength, and elasticity. In the present invention, the plastisol in the first bath must be maintained at a temperature sufficient to wet and suspend the PVC resin particles, but below the temperature at which gelation and condensation occur. Once the mold with the liquid plastisol film on its surface is removed from the bath, drain and then heat the oven to cause gelation and condensation. The exact times and temperatures for these steps depend on the particular resin, plasticizer, resin / plasticizer ratio, desired film thickness, and desired throughput for glove manufacture.
ゲル化および縮合に続き、総合PVCフィルムをその表
面上に有する型を冷やしてフィルムを強くして約75℃か
ら約90℃にフィルムを冷やす。その表面上に第一フィル
ムを有する型を第二浴槽に浸けるが、第二浴槽はポリエ
ステルポリウレタンの水性懸濁液および仕上剤を含むこ
とによりポリウレタンの第二フィルムを形成し、その
際、仕上剤は第一フィルム全体を覆う。第二浴槽は約5
から約30パーセントの固体を含むことが好ましく、そし
てバインダー、表面移動を許すスリップ剤、懸濁剤およ
び仕上剤として作用するポリエステルポリウレタンを含
むことが好ましい。好ましいポリエステルポリウレタン
は、約13から約17重量パーセントのSolucote1051 I−35
である。適切なスリップ剤は、分子量約4000から約10,0
00ドルトンの酸化ポリエチレンである。好ましい酸化ポ
リエチレンは水性エマルジョンであって、平均粒子サイ
ズ約2.5から約50ナノメーター(10-9ナノメーター)で
ある。スリップ剤は、水性エマルジョンとして約7から
約20パーセントの間で第二浴槽中に存在する。スリップ
剤は、加熱により型の表面から手袋表面をはぎとりやす
くするために機能する。仕上剤は、粒子サイズ分布約1
から約75ミクロン、好ましくは約1から約50ミクロンの
粒のそろった物質が好ましい。粒のそろった物質は、炭
化カルシウム、珪藻土、合成アルミノシリケート、ガラ
スビーズ、シリカ、合成シリケート等でありうる。仕上
剤は、約0.5から約2.0%(w/w)で第二浴槽中に存在す
る。好ましくは仕上剤は、粒子サイズ分布約1から約50
ミクロンの炭化カルシウムであり、約1%(w/w)で第
二浴槽中に存在する。第二浴槽も、分散剤、表面活性剤
および消泡剤を含むことが好ましい。第一および第二層
をその表面上に有する型を、次に第二浴槽から取り出
し、そしてオーブン中で加熱し、そして第二フィルムを
乾燥し、第一フィルムに第二フィルムを接着し、そして
型表面上に2層ユニット構造を形成する。ユニット構造
は約70℃から約90℃の間に保持され、めくり返し(cuf
f)ロールをユニット構造上に形成する。次に、外部表
面上に患者接触層および内部表面上に使用者接触層を有
する手袋を形成する型表面から該構造をはぎとり、そし
てめくり返す。Following gelation and condensation, the mold with the integrated PVC film on its surface is cooled to strengthen the film and cool the film from about 75 ° C to about 90 ° C. A mold having a first film on its surface is immersed in a second tub, the second tub comprising an aqueous suspension of polyester polyurethane and a finishing agent to form a second film of polyurethane, wherein the finishing agent Covers the entire first film. The second bathtub is about 5
And preferably about 30 percent solids, and preferably a polyester polyurethane that acts as a binder, a surface transfer slip agent, a suspending agent and a finish. Preferred polyester polyurethanes have about 13 to about 17 weight percent of Solucote 1051 I-35.
It is. Suitable slip agents have a molecular weight of about 4000 to about 10,000.
00 Dalton oxidized polyethylene. The preferred oxidized polyethylene is an aqueous emulsion, having an average particle size of about 2.5 to about 50 nanometers ( 10-9 nanometers). The slip agent is present in the second bath at between about 7 and about 20 percent as an aqueous emulsion. The slip agent functions to make it easier to remove the glove surface from the mold surface by heating. The finish has a particle size distribution of about 1
Preferred is a well-grained material from about 1 to about 50 microns, preferably from about 1 to about 50 microns. The granular material can be calcium carbide, diatomaceous earth, synthetic aluminosilicate, glass beads, silica, synthetic silicate, and the like. The finish is present in the second bath at about 0.5 to about 2.0% (w / w). Preferably, the finish has a particle size distribution of about 1 to about 50.
Micron calcium carbide, present in the second bath at about 1% (w / w). Preferably, the second bath also contains a dispersant, a surfactant and an antifoam. The mold having the first and second layers on its surface is then removed from the second bath and heated in an oven, and the second film is dried, the second film is adhered to the first film, and A two-layer unit structure is formed on the mold surface. The unit structure is maintained between about 70 ° C and about 90 ° C, and turned over (cuf
f) Form a roll on the unit structure. The structure is then stripped and flipped from the mold surface forming a glove having a patient contact layer on the outer surface and a user contact layer on the inner surface.
最終的な手袋を数えて保存カートンにパッケージする
ことが好ましい。Preferably, the final glove is counted and packaged in a storage carton.
実施例1 外部表面として手形を有する清潔な型を加熱して約70
℃から約95℃にして、約35℃から約45℃に保持されたPV
Cプラスチゾル浴槽に浸けてその表面上にPVCプラスチゾ
ルフィルムを形成した。その表面上にフィルムを有する
型を第一浴槽から取り出し、排水し、そしてオーブン中
で表面上のフィルムの温度を約160℃から約195℃にして
平均厚約0.08mmのフィルムをゲル化および縮合した。フ
ィルムを冷やして約75℃から約90℃にして、ポリウレタ
ン、スリップ剤および仕上剤を含む水性エマルジョンを
含む約35℃から約45℃に維持された第二浴槽に浸けて、
第一層上に第二層を形成した。第一層および第二層を有
する型を第二浴槽から取り出し、排水し、そして約70℃
から約90℃に加熱して乾燥し、第一層に第二層を接着す
ることによりユニット構造を形成した。めくり返し(cu
ff)をユニット構造上に形成し、手袋をはぎとってめく
り返して手袋を形成した。Example 1 A clean mold having bills as the outer surface was heated to about 70
PV maintained at about 35 ° C to about 45 ° C from about 95 ° C to about 95 ° C
It was immersed in a C plastisol bath to form a PVC plastisol film on its surface. The mold with the film on its surface is removed from the first tub, drained, and the film on the surface is gelled and condensed in an oven with an average thickness of about 0.08 mm at a temperature of about 160 ° C to about 195 ° C did. Cooling the film to about 75 ° C to about 90 ° C and immersing it in a second tub maintained at about 35 ° C to about 45 ° C containing an aqueous emulsion containing polyurethane, slip agent and finish,
A second layer was formed on the first layer. The mold with the first and second layers is removed from the second bath, drained, and
To about 90 ° C. and dried, and a unit structure was formed by bonding the second layer to the first layer. Turn over (cu
ff) was formed on the unit structure, and the glove was peeled off and turned over to form a glove.
実施例1の浴槽の組成物 実施例2 外部表面として手形を有する清潔な型を加熱して約70
℃から約95℃にして、約35℃から約45℃に保持されたPV
Cプラスチゾル浴槽に浸けてその表面上にPVCプラスチゾ
ルフィルムを形成した。その表面上にフィルムを有する
型を第一浴槽から取り出し、排水し、そしてオーブン中
で表面上のフィルムの温度を約160℃から約195℃にして
平均厚約0.08mmのフィルムをゲル化および縮合した。フ
ィルムを冷やして約75℃から約90℃にして、ポリウレタ
ン、スリップ剤および仕上剤を含む水性エマルジョンを
含む約35℃から約45℃に維持された第二浴槽に浸けて、
第一層上に第二層を形成した。第一層および第二層を有
する型を第二浴槽から取り出し、排水し、そして約70℃
から約90℃に加熱して乾燥し、第一層に第二層を接着す
ることによりユニット構造を形成した。めくり返し(cu
ff)をユニット構造上に形成し、手袋をはぎとってめく
り返して手袋を形成した。Bath composition of Example 1 Example 2 A clean mold with bills as the outer surface was heated to about 70
PV maintained at about 35 ° C to about 45 ° C from about 95 ° C to about 95 ° C
It was immersed in a C plastisol bath to form a PVC plastisol film on its surface. The mold with the film on its surface is removed from the first tub, drained, and the film on the surface is gelled and condensed in an oven with an average thickness of about 0.08 mm at a temperature of about 160 ° C to about 195 ° C did. Cooling the film to about 75 ° C to about 90 ° C and immersing it in a second tub maintained at about 35 ° C to about 45 ° C containing an aqueous emulsion containing polyurethane, slip agent and finish,
A second layer was formed on the first layer. The mold with the first and second layers is removed from the second bath, drained, and
To about 90 ° C. and dried, and a unit structure was formed by bonding the second layer to the first layer. Turn over (cu
ff) was formed on the unit structure, and the glove was peeled off and turned over to form a glove.
実施例2の浴槽の組成物 実施例3 外部表面として手形を有する清潔な型を加熱して約70
℃から約95℃にして、約35℃から約45℃に保持されたPV
Cプラスチゾル浴槽に浸けてその表面上にPVCプラスチゾ
ルフィルムを形成した。その表面上にフィルムを有する
型を第一浴槽から取り出し、排水し、そしてオーブン中
で表面上のフィルムの温度を約160℃から約195℃にして
平均厚約0.08mmのフィルムをゲル化および縮合した。フ
ィルムを冷やして約75℃から約90℃にして、ポリウレタ
ン、スリップ剤および仕上剤を含む水性エマルジョンを
含む約35℃から約45℃に維持された第二浴槽に浸けて、
第一層上に第二層を形成した。第一層および第二層を有
する型を第二浴槽から取り出し、排水し、そして約70℃
から約90℃に加熱して乾燥し、第一層に第二層を接着す
ることによりユニット構造を形成した。めくり返し(cu
ff)をユニット構造上に形成し、手袋をはぎとってめく
り返して手袋を形成した。Bathtub composition of Example 2 Example 3 A clean mold with bills as the outer surface was heated to about 70
PV maintained at about 35 ° C to about 45 ° C from about 95 ° C to about 95 ° C
It was immersed in a C plastisol bath to form a PVC plastisol film on its surface. The mold with the film on its surface is removed from the first tub, drained, and the film on the surface is gelled and condensed in an oven with an average thickness of about 0.08 mm at a temperature of about 160 ° C to about 195 ° C. did. Cooling the film to about 75 ° C to about 90 ° C and immersing it in a second tub maintained at about 35 ° C to about 45 ° C containing an aqueous emulsion containing polyurethane, slip agent and finish,
A second layer was formed on the first layer. The mold with the first and second layers is removed from the second bath, drained, and
To about 90 ° C. and dried, and a unit structure was formed by bonding the second layer to the first layer. Turn over (cu
ff) was formed on the unit structure, and the glove was peeled off and turned over to form a glove.
実施例3の浴槽の組成物 本発明の好ましい態様は以下の表2のとおりの物理特
性を有する手袋であるが、本発明は特定の用途のために
約0.035mmから約0.150mmのフィルムを形成する。Example 3 Bathtub Composition While a preferred embodiment of the present invention is a glove having the physical properties as shown in Table 2 below, the present invention forms a film from about 0.035 mm to about 0.150 mm for a particular application.
図2aおよび図2bを参照すると、ストッカムにより教示
された従来技術の模式図は接着層表面を通して突起表面
部分を有する粒子物質を有する手袋の表面を示し(図2
a)、そして比較のための本発明の表面のミクロ写真
(図2b)はポリエステルポリウレタンにより埋蔵且つ実
質的には覆われた粒子物質を有する使用者接触層の表面
を示す。 Referring to FIGS. 2a and 2b, prior art schematics taught by Stocker show the surface of a glove having particulate material with a protruding surface portion through the adhesive layer surface (FIG. 2).
a), and a microphotograph of the inventive surface for comparison (FIG. 2b) shows the surface of the user contact layer with the particulate material embedded and substantially covered by the polyester polyurethane.
本発明の手袋は、広く用いられている粉末を含むPVC
手袋例えばTru−Touch(登録商標)と同様な強度および
触質性を提供するが、粉末を用いない着用の利益を提供
する。The gloves of the present invention are made of PVC containing widely used powder.
It provides similar strength and tactility as gloves such as Tru-Touch®, but offers the benefits of wearing without powder.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B32B 5/16 B32B 5/16 27/08 27/08 (72)発明者 ヴァンデポル,マーク・イー アメリカ合衆国カリフォルニア州ロス・ ガトス,マウンテン・チャーリー・ロー ド 25150 (56)参考文献 特開 平1−221501(JP,A) 特開 昭60−119204(JP,A) 特表 平3−502529(JP,A) 米国特許3059241(US,A) 米国特許4143109(US,A) (58)調査した分野(Int.Cl.6,DB名) A41D 19/00 A41D 19/04 A61B 19/04 A61L 31/00 B29C 41/14 B32B 5/16 B32B 27/08 ──────────────────────────────────────────────────の Continuation of the front page (51) Int.Cl. 6 Identification symbol FI B32B 5/16 B32B 5/16 27/08 27/08 (72) Inventor Vandepol, Mark E Mountain, Los Gatos, California, United States of America・ Charlie Load 25150 (56) References JP-A-1-221501 (JP, A) JP-A-60-119204 (JP, A) JP-A-3-502529 (JP, A) US Patent 3052941 (US, A) U.S. Pat. No. 4,143,109 (US, A) (58) Fields investigated (Int. Cl. 6 , DB name) A41D 19/00 A41D 19/04 A61B 19/04 A61L 31/00 B29C 41/14 B32B 5/16 B32B 27/08
Claims (24)
および ポリエステルポリウレタン、約4,000から約10,000の分
子量および約25から約50ナノメーターの平均粒子サイズ
を有するスリップ剤および仕上剤を含む、第一層に接着
した第二層; からなる柔軟性製品。1. A first layer comprising a plasticized polyvinyl chloride resin;
And a polyester polyurethane, a second layer adhered to the first layer, comprising a slip agent and a finish having a molecular weight of about 4,000 to about 10,000 and an average particle size of about 25 to about 50 nanometers.
ル酸エステルからなる群から選択される可塑剤により可
塑化された縮合ポリ塩化ビニルである、請求項1記載の
柔軟性製品。2. The flexible article of claim 1, wherein the first layer is a condensed polyvinyl chloride plasticized with a plasticizer selected from the group consisting of adipic acid esters and phthalic acid esters.
成された、患者に接触する第一層;および ポリエステルポリウレタンのフィルムで形成された、患
者接触層に接着した、使用者に接触する第二層; からなる医療用2層手袋。3. A patient contacting first layer formed of a plasticized polyvinyl chloride resin film; and a user contacting second layer formed of a polyester polyurethane film and adhered to the patient contacting layer. A two-layer medical glove comprising:
フタル酸エステルからなる群から選択される可塑剤によ
り可塑化された縮合ポリ塩化ビニルにより形成されてい
る、請求項3記載の手袋。4. The glove of claim 3, wherein the patient contact layer is formed of condensed polyvinyl chloride plasticized with a plasticizer selected from the group consisting of adipic acid esters and phthalic acid esters.
mmである、請求項3記載の手袋。5. The glove has an average thickness of about 0.035 mm to about 0.150.
The glove according to claim 3, which is mm.
0の分子量および約25から約50ナノメーターの平均粒子
サイズを有するスリップ剤および仕上剤を含むことによ
りきめを有する表面を提供し、それにより使用者接触層
がそれ自体スライドして使用者の手をスライドすること
により粉末を必要とせずに容易に手袋が着用可能になる
ことを特徴とする、請求項3記載の手袋。6. The method according to claim 6, wherein the user contact layer further comprises about 4,000 to about 10,000.
By providing a textured surface by including a slip agent and a finish having a molecular weight of 0 and an average particle size of from about 25 to about 50 nanometers, the user contact layer slides itself on the user's hand. The glove according to claim 3, characterized in that the glove can be easily worn without requiring powder by sliding the glove.
リカ、ガラスビーズ、および炭化カルシウムからなる群
から選択される粒ぞろいの物質である、請求項6記載の
手袋。7. The glove according to claim 6, wherein the finishing agent is a uniform particle selected from the group consisting of amorphous synthetic silica, diatomaceous earth, silica, glass beads, and calcium carbide.
の粒子サイズ分布を有する、請求項7記載の手袋。8. The glove of claim 7, wherein the assorted material has a particle size distribution of about 1 to about 75 microns.
の粒子サイズ分布を有し、且つ炭化カルシウムからな
る、請求項8記載の手袋。9. The glove of claim 8, wherein the assorted material has a particle size distribution of about 1 to about 75 microns and comprises calcium carbide.
浴槽に表面を有する清潔な手形の型を浸け; 表面上にプラスチゾルの第一フィルムを形成し; 第一浴槽から第一フィルムを有する型を取り出し; 第一フィルムをその上に有する型を加熱してプラスチゾ
ルをゲル化および縮合し; 第一フィルムをその上に有する型を冷やし; ポリエステルポリウレタン、約4,000から約10,000の分
子量および約25から約50ナノメーターの平均粒子サイズ
を有するスリップ剤および仕上剤を含む水性懸濁液を含
む第二浴槽に、表面上に第一フィルムを有する型を浸
け; 表面上に第一フィルムおよび第二フィルムを有する型を
第二浴槽から取り出し; 第一フィルムおよび第二フィルムを有する型を加熱する
ことにより乾燥させ且つ第一フィルムと第二フィルムを
接着し、そして型の表面上に2層ユニット構造を形成
し; 型上の2層ユニット構造上でめくり返しを形成し;そし
て 型からユニット構造をはぎとりそしてめくり返すことに
より外部表面上に患者接触層そして内部表面上に使用者
接触層を有する手袋を形成する 工程からなる、医療用手袋の製造方法。10. Dipping a clean handprint mold having a surface in a first bath containing polyvinyl chloride plastisol; forming a first film of plastisol on the surface; removing the mold having the first film from the first bath. Heating the mold having the first film thereon to gel and condense the plastisol; cooling the mold having the first film thereon; polyester polyurethane, molecular weight of about 4,000 to about 10,000 and about 25 to about 50; Immerse the mold having the first film on the surface in a second bath containing an aqueous suspension containing a slip agent and a finish having an average particle size of nanometers; having the first film and the second film on the surface The mold is removed from the second bath; the mold having the first and second films is dried by heating and the first and second films are removed. Gluing and forming a two-layer unit structure on the surface of the mold; forming a flip on the two-layer unit structure on the die; and patient contact on the outer surface by peeling and flipping the unit structure from the die Forming a glove having a layer and a user contact layer on the inner surface.
に、さらに計数工程およびパッケージング工程を含む、
請求項10記載の方法。11. The method according to claim 11, further comprising a counting step and a packaging step after the step of stripping and turning over.
The method according to claim 10.
塩化ビニルコポリマーからなる群から選択される樹脂、
および可塑剤、安定剤、増粘剤および発色剤により形成
される液体プラスチゾルを含む、請求項10記載の方法。12. The resin of claim 1 wherein the first bath is a resin selected from the group consisting of polyvinyl chloride and polyvinyl chloride copolymer.
11. The method according to claim 10, comprising a liquid plastisol formed by a plasticizer, a stabilizer, a thickener and a color former.
ら約1.2:1である、請求項12記載の方法。13. The method of claim 12, wherein the ratio of resin to plasticizer is from about 0.8: 1 to about 1.2: 1.
ルポリウレタンエマルジョン、仕上剤、懸濁剤および湿
潤剤を含む、請求項10記載の方法。14. The method of claim 10, wherein the second bath contains an aqueous anionic polyester polyurethane emulsion, a finish, a suspending agent and a wetting agent.
95重量パーセントの水を含む、請求項14記載の方法。15. The method according to claim 15, wherein the second bathtub comprises from about 70 weight percent to about
15. The method of claim 14, comprising 95 weight percent water.
シリカ、ガラスビーズ、および炭化カルシウムからなる
群から選択される粒ぞろいの物質である、請求項14記載
の方法。(16) a finishing agent comprising amorphous synthetic silica, diatomaceous earth,
15. The method according to claim 14, wherein the material is a uniform material selected from the group consisting of silica, glass beads, and calcium carbide.
ンの粒子サイズ分布を有する炭化カルシウムからなる、
請求項16記載の方法。17. The material of the assortment comprises calcium carbide having a particle size distribution of about 1 to about 50 microns.
17. The method according to claim 16.
プラスチゾルの第一層を形成し; ポリエステルポリウレタン、約4,000から約10,000の分
子量および約25から約50ナノメーターの平均粒子サイズ
を有するスリップ剤および仕上剤を含む第二層を第一層
に接着させて形成する; 工程からなる、医療用手袋の製造方法。18. A first layer of polyvinyl chloride plastisol formed on the outer surface of the bill mold; polyester polyurethane, a slip having a molecular weight of about 4,000 to about 10,000 and an average particle size of about 25 to about 50 nanometers. Forming a second layer containing an agent and a finishing agent by adhering to the first layer.
粘度数を有するポリ塩化ビニル、およびフタル酸エステ
ルおよびアジピン酸エステルおよびジエステルおよびそ
れらのブレンドからなる群から選択される可塑剤を含
む、請求項18記載の方法。19. The plastisol comprises polyvinyl chloride having an intrinsic viscosity of about 0.7 to about 1.5, and a plasticizer selected from the group consisting of phthalates and adipic esters and diesters and blends thereof. Item 18. The method according to Item 18.
よび発色剤を含み、プラスチゾルがプラスチゾルに対す
る樹脂の比率約0.8:1.0から約1.0:1.2を有し、そして第
一層を有する型を加熱する工程を含むことによりプラス
チゾルをゲル化および縮合する、請求項18記載の方法。20. The plastisol further comprises a thickener, a stabilizer and a color former, the plastisol has a ratio of resin to plastisol of about 0.8: 1.0 to about 1.0: 1.2, and heats the mold having the first layer. 19. The method of claim 18, wherein the step comprises gelling and condensing the plastisol.
約70パーセントから約95パーセントの水、スリップ剤、
粘度制御剤、消泡剤および湿潤剤を含む、請求項18記載
の方法。21. The bath for forming the second layer may further comprise from about 70 percent to about 95 percent of water, a slip agent,
19. The method according to claim 18, comprising a viscosity controlling agent, an antifoaming agent and a wetting agent.
ラスビーズ、シリカおよび非晶性合成シリカからなる群
から選択される粒ぞろいの物質であり、そして、粒ぞろ
いの物質が約1から約50ミクロンの粒子サイズ分布を有
する、請求項21記載の方法。22. The finish is a homogenous material selected from the group consisting of calcium carbide, diatomaceous earth, glass beads, silica and amorphous synthetic silica, and wherein the homogenous material is from about 1 to about 50 microns. 22. The method of claim 21 having a particle size distribution.
り乾燥させ且つ第一層に接着して型の表面上にユニット
構造を形成する、請求項18記載の方法。23. The method of claim 18, wherein the second layer is dried by heating in an oven and adheres to the first layer to form a unitary structure on the surface of the mold.
形成し、型から構造をはぎとりめくり返すことにより手
袋を形成する、請求項18記載の方法。24. The method of claim 18, further comprising forming a turn over the unit structure and stripping the structure from the mold to form a glove.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US172,453 | 1993-12-23 | ||
US08/172,453 | 1993-12-23 | ||
US08/172,453 US5881386A (en) | 1993-12-23 | 1993-12-23 | Flexible polyvinyl chloride article and method of making |
PCT/US1994/014482 WO1995017107A1 (en) | 1993-12-23 | 1994-12-16 | Flexible polyvinyl chloride article and method of making |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH08505911A JPH08505911A (en) | 1996-06-25 |
JP2871099B2 true JP2871099B2 (en) | 1999-03-17 |
Family
ID=22627755
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51750995A Expired - Fee Related JP2871099B2 (en) | 1993-12-23 | 1994-12-16 | Flexible polyvinyl chloride product and method for producing the same |
Country Status (9)
Country | Link |
---|---|
US (1) | US5881386A (en) |
EP (1) | EP0686004B2 (en) |
JP (1) | JP2871099B2 (en) |
AT (1) | ATE177600T1 (en) |
AU (1) | AU1373095A (en) |
CA (1) | CA2156524C (en) |
DE (1) | DE69417218T3 (en) |
FI (1) | FI953931A0 (en) |
WO (1) | WO1995017107A1 (en) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5590420A (en) * | 1994-03-24 | 1997-01-07 | Gunn; Robert T. | Low friction apparel |
US6730380B2 (en) | 1996-02-20 | 2004-05-04 | Safeskin Corp. | Readily-donned elastomeric articles |
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-
1993
- 1993-12-23 US US08/172,453 patent/US5881386A/en not_active Expired - Lifetime
-
1994
- 1994-12-16 WO PCT/US1994/014482 patent/WO1995017107A1/en active IP Right Grant
- 1994-12-16 EP EP95904924A patent/EP0686004B2/en not_active Expired - Lifetime
- 1994-12-16 CA CA 2156524 patent/CA2156524C/en not_active Expired - Lifetime
- 1994-12-16 DE DE1994617218 patent/DE69417218T3/en not_active Expired - Lifetime
- 1994-12-16 AU AU13730/95A patent/AU1373095A/en not_active Abandoned
- 1994-12-16 AT AT95904924T patent/ATE177600T1/en not_active IP Right Cessation
- 1994-12-16 JP JP51750995A patent/JP2871099B2/en not_active Expired - Fee Related
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1995
- 1995-08-22 FI FI953931A patent/FI953931A0/en not_active Application Discontinuation
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CA2156524A1 (en) | 1995-06-29 |
WO1995017107A1 (en) | 1995-06-29 |
DE69417218D1 (en) | 1999-04-22 |
DE69417218T2 (en) | 1999-09-30 |
JPH08505911A (en) | 1996-06-25 |
ATE177600T1 (en) | 1999-04-15 |
EP0686004A4 (en) | 1996-03-06 |
DE69417218T3 (en) | 2005-08-11 |
US5881386A (en) | 1999-03-16 |
EP0686004A1 (en) | 1995-12-13 |
FI953931A (en) | 1995-08-22 |
EP0686004B1 (en) | 1999-03-17 |
EP0686004B2 (en) | 2004-12-15 |
FI953931A0 (en) | 1995-08-22 |
AU1373095A (en) | 1995-07-10 |
CA2156524C (en) | 2000-08-01 |
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